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Variant (rsID / SNP)

rs216195

SMG6

rs216195 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SMG6. Location: chromosome 17, position 2,203,167. The table records no clinical significance for this variant.

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Reference-table entries

SMG6Not classified
Variant type
missense_variant
Chromosome / position
17:2203167
HGVS
NM_017575.5,c.880A>C,p.Lys294Gln
Allele change
Missense_K294Q

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.